Disease #05587

Official abbreviation FAME3;FMCTE3
Name epilepsy, myoclonic, familial adult, type 3 (FAME3, FMCTE3)
OMIM ID 613608
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MARCH6
Associated tissues -
Disease features autosomal dominant
Remarks -